MOMETASONE FUROATE

Product NDC

70518-0961

11-digit product format

705180961

Labeler code

70518

Product ID

70518-0961_67f2fb2b-499b-8637-e053-2991aa0a3c5c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

MOMETASONE FUROATE

Dosage form

SPRAY, METERED

Route

NASAL

Labeler

REMEDYREPACK INC.

Application

ANDA091161

Marketing category

ANDA

Marketing start

2018-03-20

Marketing end

0000-00-00

Substance

MOMETASONE

Active strength

50 ug/1

Pharmacologic classes

Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Corticosteroid Hormone Receptor Agonists [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record